Wound healing is a complex process that, involves inflammation, apoptosis,
growth, and tissue remodeling. The autoimmune-prone inbred mouse strain MRL
/+ manifests accelerated and extensive healing to ear punch wounds, suggest
ing a Pink between immune defects and wound healing. Prior studies with lup
us-prone mice have shown that hematopoietic cells of lupus-prone strains ca
n transfer disease to otherwise non-autoimmune-prone recipients. In this st
udy we performed reciprocal bone marrow transfers between MRL and the contr
ol strain B10.BR and found that radioresistant MRL/+ host cells, rather tha
n hematopoietic cells, are required for the healing response. Ww have also
made the novel observations that, compared to normal controls, MRL/+ hemato
poietic cells overproduce TGF-beta 1 and manifest impaired inflammatory res
ponses to lipopolysaccharide challenge. These features suggest that the abe
rrant wound healing phenotype of MRL mice is independent of their propensit
y to develop autoimmunity. (C) 1999 Academic Press.